Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP820532.RATJ-Hf3yD4JtgMx6Mmxts1cYRUvK50az2Cwvr9SjfX20130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP820532.RATJ-Hf3yD4JtgMx6Mmxts1cYRUvK50az2Cwvr9SjfX20130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP820532.RATJ-Hf3yD4JtgMx6Mmxts1cYRUvK50az2Cwvr9SjfX20130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP820532.RATJ-Hf3yD4JtgMx6Mmxts1cYRUvK50az2Cwvr9SjfX20130_provenance.
- befree-2016 importedOn "2016-02-19" NP820532.RATJ-Hf3yD4JtgMx6Mmxts1cYRUvK50az2Cwvr9SjfX20130_provenance.
- NP820532.RATJ-Hf3yD4JtgMx6Mmxts1cYRUvK50az2Cwvr9SjfX20130_assertion wasGeneratedBy ECO_0000203 NP820532.RATJ-Hf3yD4JtgMx6Mmxts1cYRUvK50az2Cwvr9SjfX20130_provenance.
- NP820532.RATJ-Hf3yD4JtgMx6Mmxts1cYRUvK50az2Cwvr9SjfX20130_assertion wasDerivedFrom befree-2016 NP820532.RATJ-Hf3yD4JtgMx6Mmxts1cYRUvK50az2Cwvr9SjfX20130_provenance.
- NP820532.RATJ-Hf3yD4JtgMx6Mmxts1cYRUvK50az2Cwvr9SjfX20130_assertion SIO_000772 20569259 NP820532.RATJ-Hf3yD4JtgMx6Mmxts1cYRUvK50az2Cwvr9SjfX20130_provenance.
- NP820532.RATJ-Hf3yD4JtgMx6Mmxts1cYRUvK50az2Cwvr9SjfX20130_assertion evidence source_evidence_literature NP820532.RATJ-Hf3yD4JtgMx6Mmxts1cYRUvK50az2Cwvr9SjfX20130_provenance.
- NP820532.RATJ-Hf3yD4JtgMx6Mmxts1cYRUvK50az2Cwvr9SjfX20130_assertion description "[Thirty-four cases of SDS patients were analyzed and compared to other patients with the four most common IBMFSs on the CIMFS: Diamond Blackfan anemia, Fanconi anemia (FA), Kostmann/severe congenital neutropenia and dyskeratosis congenita (DC).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP820532.RATJ-Hf3yD4JtgMx6Mmxts1cYRUvK50az2Cwvr9SjfX20130_provenance.